Ciprofloxacin

Product NDC
67296-0579
11-digit product format
672960579
Labeler code
67296
Product ID
67296-0579_98eb16dd-de60-471b-a2da-dc9334f7e409
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
RedPharm Drug Inc.
Application
ANDA077859
Marketing category
ANDA
Marketing start
2009-08-01
Marketing end
0000-00-00
Substance
CIPROFLOXACIN
Active strength
500 mg/1
Pharmacologic classes
Quinolone Antimicrobial [EPC],Quinolones [CS]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ea50b939-d92a-4100-84f5-1c1089663837Product name220240705
90aab9f8-63f3-478d-8db8-951525a18ab1Product name120180814
200e1d3d-46da-4371-beed-747da3cb3ff8Product name120180702
9e453f34-aacb-44d5-a119-c0e3dc1fca2aProduct name120160622
01eecbfe-0b50-413b-8898-6905c89b6568Product name120151228
a3304bb6-ef4e-06df-d604-35f7e883ed6cProduct name120140508
abaf203f-619e-f265-559f-8c81af5cb1c2Product name120140508
de5ea793-ffd9-0308-b0ca-00d9967be4eeProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67296-0579-22020-01-31C16284748780-19d75b9d0-76e4-f424-e053-dadaa90a57ceCiproflaxin Tablets

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-0579-2Ciprofloxacin10 in 1 BOTTLETABLET, FILM COATED101

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CIPROFLOXACINACTIVE INGREDIENT5E8K9I0O4UCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
CIPROFLOXACINACTIVE MOIETY5E8K9I0O4UCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
HYPROMELLOSE 2910 (5 MPA.S)INACTIVE INGREDIENTR75537T0T4CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
POVIDONE K30INACTIVE INGREDIENTU725QWY32XCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67296-0579CIPROFLOXACIN TABLET, FILM COATED [REDPHARM DRUG INC.]1Legacy NDC, 1 package rows20110628_6d8d72fe-e89c-4e08-9ca1-ec64c4890205.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
309309ciprofloxacin 500 MG Oral TabletPSN6d8d72fe-e89c-4e08-9ca1-ec64c48902051
309309ciprofloxacin 500 MG Oral TabletSCD6d8d72fe-e89c-4e08-9ca1-ec64c48902051
309309ciprofloxacin (as ciprofloxacin HCl) 500 MG Oral TabletSY6d8d72fe-e89c-4e08-9ca1-ec64c48902051

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
67296-0579-26729605790210 in 1 BOTTLEHistorical